Canonical Allele Identifier: CA2744009060
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68430115_68430116insACT , CM000663.2:g.68430115_68430116insACT GRCh38
NC_000001.10:g.68895798_68895799insACT , CM000663.1:g.68895798_68895799insACT GRCh37
NC_000001.9:g.68668386_68668387insACT NCBI36
NG_008472.1:g.24844_24845insAGT
NG_008472.2:g.24844_24845insAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1451-189_1451-188insAGT MANE Select ENSP00000262340.5:n.1451-189_1451-188insAGT
ENST00000262340.5:c.1451-189_1451-188insAGT ENSP00000262340.5:n.1451-189_1451-188insAGT
NM_000329.2:c.1451-189_1451-188insAGT NP_000320.1:n.1451-189_1451-188insAGT
XM_017002027.1:c.1175-189_1175-188insAGT XP_016857516.1:n.1175-189_1175-188insAGT
NM_000329.3:c.1451-189_1451-188insAGT MANE Select NP_000320.1:n.1451-189_1451-188insAGT